TY - JOUR
T1 - El papel de los polimorfismos genéticos del receptor de vitamina d en la obesidad
T2 - una revisión sistemática y un metanálisis
AU - Yuliawati, Tri Hartini
AU - Sari, Dewi Ratna
AU - Wungu, Citrawati Dyah Kencono
AU - Faizah, Zakiyatul
AU - Hamidah, Berliana
AU - Amanda, Bella
AU - Prasetiowati, Lucky
AU - Rimbun,
AU - Purwantari, Kusuma Eko
AU - Darsini, Ninik
AU - Ashari, Faisal Yusuf
AU - Taib, Wan Rohani Wan
AU - Alwi, Zilfalil Bin
N1 - Publisher Copyright:
© 2025; Los autores.
PY - 2025
Y1 - 2025
N2 - Introduction: obesity has become a major global issue since it can increase the risk of fatal disease. Genetic variation in the vitamin D receptor (VDR) gene is a potential candidate for obesity, though findings are inconclusive. Objectives: this meta-analysis aims to determine the association between VDR polymorphisms and obesity risk. Method: all relevant studies from 1990 to January 2024 were screened using PubMed, Web of Science, Science Direct, and Scopus. This meta-analysis included studies meeting PROSPERO-registered eligibility criteria. Pooled odds ratios (OR) with 95 % confidence intervals (CI) for six VDR gene polymorphisms (BsmI, FokI, TaqI, ApaI, and Cdx2) were generated using RevMan 5.4. Results: this meta-analysis included 23 studies with 5715 obese/overweight and 4887 non-obese individuals from China, Malaysia, Egypt, Turkey, India, Iran, UAE, Saudi Arabia, Czech Republic, Greece, USA, Denmark, Hungary, and Belgium. The findings show an association between VDR ApaI polymorphism and reduced obesity risk in homozygous models [aa vs. AA: OR=0,76, CI=0,60-0,97; P=0,03]. The TaqI variant is linked to increased obesity risk in Europeans under allelic [t vs. T: OR=1,33, CI=1,11-1,60; P=0,002], homozygous [tt vs. TT: OR=1,68, CI=1,13-2,50; P=0,010], dominant [tt vs. TT+Tt: OR=1,47, CI=1,07-2,03; P=0,02], and recessive [Tt+tt vs. TT: OR=1,43, CI=1,08-1,89; P=0,01] models. Conclusions: this meta-analysis suggests the aa genotype of VDR ApaI polymorphism may protect against obesity across populations. In Europeans, the t allele of VDR TaqI polymorphism is identified as an obesity risk factor.
AB - Introduction: obesity has become a major global issue since it can increase the risk of fatal disease. Genetic variation in the vitamin D receptor (VDR) gene is a potential candidate for obesity, though findings are inconclusive. Objectives: this meta-analysis aims to determine the association between VDR polymorphisms and obesity risk. Method: all relevant studies from 1990 to January 2024 were screened using PubMed, Web of Science, Science Direct, and Scopus. This meta-analysis included studies meeting PROSPERO-registered eligibility criteria. Pooled odds ratios (OR) with 95 % confidence intervals (CI) for six VDR gene polymorphisms (BsmI, FokI, TaqI, ApaI, and Cdx2) were generated using RevMan 5.4. Results: this meta-analysis included 23 studies with 5715 obese/overweight and 4887 non-obese individuals from China, Malaysia, Egypt, Turkey, India, Iran, UAE, Saudi Arabia, Czech Republic, Greece, USA, Denmark, Hungary, and Belgium. The findings show an association between VDR ApaI polymorphism and reduced obesity risk in homozygous models [aa vs. AA: OR=0,76, CI=0,60-0,97; P=0,03]. The TaqI variant is linked to increased obesity risk in Europeans under allelic [t vs. T: OR=1,33, CI=1,11-1,60; P=0,002], homozygous [tt vs. TT: OR=1,68, CI=1,13-2,50; P=0,010], dominant [tt vs. TT+Tt: OR=1,47, CI=1,07-2,03; P=0,02], and recessive [Tt+tt vs. TT: OR=1,43, CI=1,08-1,89; P=0,01] models. Conclusions: this meta-analysis suggests the aa genotype of VDR ApaI polymorphism may protect against obesity across populations. In Europeans, the t allele of VDR TaqI polymorphism is identified as an obesity risk factor.
KW - Genetics
KW - Meta-Analysis
KW - Obesity
KW - Polymorphism
KW - Vitamin D Receptor
UR - http://www.scopus.com/inward/record.url?scp=85210438228&partnerID=8YFLogxK
U2 - 10.56294/saludcyt20251072
DO - 10.56294/saludcyt20251072
M3 - Article
AN - SCOPUS:85210438228
SN - 2796-9711
VL - 5
JO - Salud, Ciencia y Tecnologia
JF - Salud, Ciencia y Tecnologia
M1 - 1072
ER -